4.5 Review

Neuronal vs glial glutamate uptake: Resolving the conundrum

期刊

NEUROCHEMISTRY INTERNATIONAL
卷 98, 期 -, 页码 29-45

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuint.2016.05.009

关键词

Glutamate uptake; EAAT2; Glutamate transporter; Conditional knockout; Synaptosomes; Axon-terminals

资金

  1. Norwegian Research Council [240844]
  2. Novo Nordisk Fonden [NNF14OC0010959]
  3. Novo Nordisk Fonden [NNF15OC0016528, NNF14OC0010959] Funding Source: researchfish

向作者/读者索取更多资源

Neither normal brain function nor the pathological processes involved in neurological diseases can be adequately understood without knowledge of the release, uptake and metabolism of glutamate. The reason for this is that glutamate (a) is the most abundant amino acid in the brain, (b) is at the cross-roads between several metabolic pathways, and (c) serves as the major excitatory neurotransmitter. In fact most brain cells express glutamate receptors and are thereby influenced by extracellular glutamate. In agreement, brain cells have powerful uptake systems that constantly remove glutamate from the extracellular fluid and thereby limit receptor activation. It has been clear since the 1970s that both astrocytes and neurons express glutamate transporters. However the relative contribution of neuronal and glial transporters to the total glutamate uptake activity, however, as well as their functional importance, has been hotly debated ever since. The present short review provides (a) an overview of what we know about neuronal glutamate uptake as well as an historical description of how we got there, and (b) a hypothesis reconciling apparently contradicting observations thereby possibly resolving the paradox. (C) 2016 Elsevier Ltd. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据